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U.S. Department of Health and Human Services

Premarket Approval (PMA)
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Note: this medical device record is a supplement. The device description may have changed. Be sure to look at the original PMA to get an up-to-date view of this device.
 
Trade NameMODEL 3003 PROGRAMMER MODEL 3036B FUNCTION PACK
Classification Nameimplantable pacemaker pulse-generator
Generic Namepulse generator programmer function pack
Regulation Number870.3610
ApplicantPACESETTER SYSTEMS
PMA NumberP880086
Supplement NumberS001
Date Received08/25/1989
Decision Date05/04/1990
Product Code
DXY[ Registered Establishments with DXY ]
Advisory Committee Anesthesiology
Supplement Typenormal 180 day track
Supplement Reason change design/components/specifications - other
Expedited Review Granted? No
Combination Product No
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